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FDA 510(k)

SENSITITRE 18 HOUR SUSCEPTIBILITY PLATES

K-Number: K960235 · 1996-03-27

Decision Date1996-03-27
Product CodeJWY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SENSITITRE 18 HOUR SUSCEPTIBILITY PLATES is the device name listed in this FDA 510(k) record. The listed applicant is Accumed Intl., Inc.. It received FDA 510(k) clearance on 1996-03-27 under 510(k) number K960235. The device is classified under product code JWY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SENSITITRE 18 HOUR SUSCEPTIBILITY PLATES?

SENSITITRE 18 HOUR SUSCEPTIBILITY PLATES is a medical device that received FDA 510(k) clearance on 1996-03-27. The listed applicant is Accumed Intl., Inc.. The 510(k) number is K960235.

When did SENSITITRE 18 HOUR SUSCEPTIBILITY PLATES receive FDA 510(k) clearance?

SENSITITRE 18 HOUR SUSCEPTIBILITY PLATES received FDA 510(k) clearance on 1996-03-27, under 510(k) number K960235.

Who is the listed applicant for SENSITITRE 18 HOUR SUSCEPTIBILITY PLATES?

The FDA 510(k) record lists Accumed Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SENSITITRE 18 HOUR SUSCEPTIBILITY PLATES?

The FDA product code for SENSITITRE 18 HOUR SUSCEPTIBILITY PLATES is JWY.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Accumed Intl., Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 12 devices →

Related Devices (Code: JWY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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